Canonical Allele Identifier: PA339526
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216793
ClinVar RCV Id: RCV000200748 RCV000408962 RCV000410527 RCV000567218 RCV003316114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe934Val
CA339524
NM_032043.3:c.2800T>G